Variant #0001781808 (NC_000019.9:g.45866982G>A, NC_000019.9(NM_000400.3):c.1118+19C>T (ERCC2))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.45866982G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC2_000174
Frequency 1/10048
Freq. EA 0/6740
Freq. AA 1/3308
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 01:48:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 ?/? c.1118+19C>T r.(=) p.(=)